Little Mix alum Jesy Nelson’s 8-month-old twins diagnosed with severe muscle disease, may never walk

Jesy Nelson's World Turns Darkest as Twins Diagnosed with Rare Muscular Disease

Pop sensation Jesy Nelson, who rose to fame with girl group Little Mix, has been left reeling after her eight-month-old twin daughters were diagnosed with a rare and devastating neuromuscular disorder called Spinal Muscular Atrophy (SMA) Type 1.

The 34-year-old singer-songwriter broke down in tears while sharing the heartbreaking news on Instagram, revealing that doctors have told her babies Ocean Jade and Story Monroe may never walk or regain neck strength, leaving them with significant disabilities. "We were told they're probably never going to be able to walk... they probably will never regain their neck strength so they will be disabled," Nelson said, her voice shaking with emotion.

SMA is a genetic condition that causes progressive muscle weakness, leading to wasting of certain muscles over time. According to the Cleveland Clinic, there is no cure for SMA, but therapies and medications can help manage symptoms. The condition is considered one of the most severe muscular diseases a baby can develop, and its progression can be rapid.

Nelson had initially flagged some concerns with her daughters' movement after just a few months old, which led to their diagnosis at eight months. Her mother noticed that the twins were not showing as much movement in their legs as they should have been. "A few signs then started to show a bit later on that they were struggling to feed properly," Nelson recalled. She urged parents to be vigilant and seek medical attention immediately if they notice any concerning symptoms.

The diagnosis has left Nelson feeling overwhelmed, with her babies requiring constant treatment and care. "If it's not treated in time, your baby's life expectancy will not make it past the age of 2," she warned, highlighting the importance of early intervention.

Nelson's journey as a mother has taken a dramatic turn since welcoming her twins, Ocean Jade and Story Monroe, in May 2025. After facing backlash over her appearance and singing style in 2021, she took a step back from the spotlight before returning with her new family. However, this latest development has left fans and friends in shock, as they try to come to terms with the challenges that lie ahead for the young mother and her babies.
 
😔 I feel so bad for Jesy Nelson, she's already been through so much after her struggles in the spotlight and now this news is just heartbreaking. As a parent myself, it's hard to imagine going through what she's going through right now. The thought of her babies not being able to walk or regain neck strength is devastating. I hope they receive the best care possible and that therapy and meds can help manage their symptoms. 🤞
 
OMG, my heart is literally breaking for Jesy 💔👶️ She's already been through so much with all the drama and whatnot, but to have this happen to her tiny munchkins? 😱 It's just too much. I feel like she's going to lose it completely 🤯 SMAs Type 1 is no joke, and it's devastating that these little ones might not get to experience some basic things like walking or even just being able to hold their heads up 🙏

I know the medical team is trying to help them with therapy and meds and all that, but as a mom, you want your babies to be healthy and happy, you know? 💕 And the thing that's scaring her is that they might not live past 2 years old... 😨 That's just heartbreaking. I'm sending all my love to Jesy and her little ones, and to all the parents out there who are going through this too 🤗
 
😱🤕 I'm literally shook for Jesy Nelson right now! 💔 Her twin babies' diagnosis is so heartbreaking 😭. I can only imagine how scary it must be for her as a new mom 🤰♀️. It's amazing that she's being open and honest about the situation, but also so brave to share the struggles of dealing with SMA Type 1 🙏. Fans are rallying around her with love and support #TeamJesy 💕, but it's clear that this diagnosis has turned her world upside down 😵. As a mom myself, I can only imagine how overwhelming it must be to care for two tiny humans with such serious needs 🤯. Sending all my positive vibes and prayers to Jesy Nelson and her babies ❤️ #SMAawareness #NewMomLife #SupportJesy 💖
 
OMG I CANT EVEN RIGHT NOW 🤯👧👦 Jesy Nelson is going through so much and I can only imagine how hard it must be for her as a mom to deal with this diagnosis for her twin babies 🤕 The fact that they may never walk or regain neck strength is just heartbreaking 😭 And the thing is SMA is super rare but also super devastating for parents who are already dealing with so much stress and worry 💔 I feel like there's gotta be more research being done on this condition ASAP so we can find a cure or at least some way to manage the symptoms 🤞
 
😱 I'm literally shook thinking about Jesy's daughters going through this... SMA Type 1 is just so rare & devastating 🤕. As a parent myself (just an online one lol), I can only imagine how scary it must be to receive news like that & have no control over the outcome 🙅‍♀️. The fact that they might never walk or regain neck strength... *sigh* 💔 It's heartbreaking, but I'm so proud of Jesy for being open about her journey & using her platform to raise awareness about SMA 👏. We gotta support her & her babies through this tough time 🤗💕
 
🤕 oh no, poor jesy nelson 🙏 she's already been through so much in 2025 and now this... but you know what? i think she's going to be an amazing mom 👩‍👧‍👦 to these little munchkins despite everything. we should all be supporting her & sending love 🌈 to ocean jade & story monroe 🤗 i'm sure they'll bring so much joy into her life, even if they do have some health challenges ahead of them 💖
 
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